A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436381



Internal ID21093934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70412401..70414300hg38UCSC Ensembl
chr9:73027317..73029216hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227421
Samples
Known GenesKLF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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